Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 13:113122874 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM025192

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_014162

HGVS names

This variant has 14 HGVS names - Show

About this variant

Variant displays